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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 420463생성일: 2026년 10월 26일

Pyridine → 2-Pyridinecarboxamide

https://huagongshe.com/reaction/420463

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물O-PhenylenediamineHCID 7243—
반응물Picolinoyl Chloride HydrochlorideHCID 135033—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매Ethyl AcetateHCID 8857—
생성물2-PyridinecarboxamideHCID 1507060%

반응 단계

Dissolving 5.0 g (17 mmol) of (4-bromo-phenyl)-(2-nitrophenyl)-amine into 50 milliliter of tetrahydrofuran, an aqueous solution prepared by dissolving 15 g (86 mmol) of sodium dithionite into 60 milliliter of water was added. Subsequently, adding 10 milliliter of methanol, the resultant solution was stirred at room temperature for 3 hours. After recognizing that the color (orange) of the resultant solution almost disappeared, water was added, followed by extracting with ethyl acetate. After sufficiently drying an organic layer with sodium sulfate, the solvent was removed by distillation, and as a result, phenylenediamine was obtained. Dissolving the resultant phenylenediamine into 150 milliliter of ethyl acetate, an organic layer was extracted. Further, 5.4 g (68 mmol) of pyridine, 3.6 g (23 mmol) of 2-picolinic acid chloride hydrochloride and catalyst amount of 4-dimethylaminopyridine (DMAP) were added to the organic layer, and the resultant solution was stirred at room temperature for 3 hours, followed by left standing for a night. After completion of the reaction, adding water, separation with filtration was carried out for precipitated solids and then, they were sufficiently washed with water and methanol, thereby obtaining 3.8 g of 2-picolinic acid amide as white solid (yield: 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08097349B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-ecbca9b7a3d24e138b1f1cf05f63770c
출처 메모uspto-grants-2012_01